CJ/T 3050-1995 喷泉喷头

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基本信息
标准名称:喷泉喷头
英文名称:Fountain nozzles
中标分类: 建材 >> 公用与市政建设器材设备 >> 园林动植物及其器材
替代情况:被CJ/T 209-2005代替
发布日期:1995-12-13
实施日期:1994-12-01
首发日期:
作废日期:2005-10-01
归口单位:建设部城镇建设标准技术归口单位建设部城市建设研究院
起草单位:建设部城镇建设标准技术归口单位建设部城市建设研究院
出版日期:
页数:17页
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所属分类: 建材 公用与市政建设器材设备 园林动植物及其器材
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【英文标准名称】:StandardPracticeforSelectingGenericBiologicalTestMethodsforMaterialsandDevices
【原文标准名称】:材料和装置用一般生物试验方法的选择的标准实施规程
【标准号】:ASTMF748-2006(2010)
【标准状态】:现行
【国别】:美国
【发布日期】:2006
【实施或试行日期】:
【发布单位】:美国材料与试验协会(US-ASTM)
【起草单位】:F04.16
【标准类型】:(Practice)
【标准水平】:()
【中文主题词】:
【英文主题词】:animaltesting;biocompatibility;invivotesting;laboratorytesting;toxicity;Biocompatibility
【摘要】:Theobjectiveofthispracticeistorecommendsufficientbiologicaltestingtoestablishareasonablelevelofconfidenceconcerningthebiologicalresponsetoamaterialordevice,whileatthesametimeavoidingunnecessarytesting.Thispracticeisintendedtoprovideguidancetothematerialsinvestigatorinselectingtheproperprocedurestobecarriedoutforthescreeningofnewormodifiedmaterials.Becauseeachmaterialandeachimplantsituationinvolvesitsownuniquecircumstances,theserecommendationsshouldbemodifiedasnecessaryanddonotconstitutetheonlytestingthatwillberequiredforamaterialnorshouldtheseguidelinesbeinterpretedasminimumrequirementsforanyparticularsituation.Whileanattempthasbeenmadetoproviderecommendationfordifferentimplantcircumstances,someoftherecommendedtestingmaynotbenecessaryorreasonableforaspecificmaterialorapplication.1.1Thispracticerecommendsgenericbiologicaltestmethodsformaterialsanddevicesaccordingtoend-useapplications.Whilechemicaltestingforextractableadditivesandresidualmonomersorresiduesfromprocessingaidsisnecessaryformostimplantmaterials,suchtestingisnotincludedaspartofthispractice.Thereaderiscautionedthattheareaofmaterialsbiocompatibilitytestingisarapidlyevolvingfield,andimprovedmethodsareevolvingrapidly,sothispracticeisbynecessityonlyaguideline.Athoroughknowledgeofcurrenttechniquesandresearchiscriticaltoacompleteevaluationofnewmaterials.1.2Thesetestprotocolsareintendedtoapplytomaterialsandmedicaldevicesforhumanapplication.Biologicalevaluationofmaterialsanddevices,andrelatedsubjectssuchaspyrogentesting,batchtestingofproductionlots,andsoon,arealsodiscussed.Testsincludethoseperformedonmaterials,endproducts,andextracts.Rationaleandcommentsoncurrentstateoftheartareincludedforalltestproceduresdescribed.1.3Thebiocompatibilityofmaterialsusedinsingleormulticomponentmedicaldevicesforhumanusedependstoalargedegreeontheparticularnatureoftheend-useapplication.Biologicalreactionsthataredetrimentaltothesuccessofamaterialinonedeviceapplicationmayhavelittleornobearingonthesuccessfuluseofthematerialforadifferentapplication.Itis,therefore,notpossibletospecifyasetofbiocompatibilitytestmethodswhichwillbenecessaryandsufficienttoestablishbiocompatibilityforallmaterialsandapplications.1.4Theevaluationoftissueengineeredmedicalproducts(TEMPs)may,insomecases,involvedifferentoradditionaltestingbeyondthosesuggestedfornon-tissue-basedmaterialsanddevices.Whereappropriate,thesedifferencesarediscussedinthispracticeandadditionaltestsdescribed.1.5Theethicaluseofresearchanimalsplacestheobligationontheindividualinvestigatortodeterminethemostefficientmethodsforperformingthenecessarytestingwithoutundueuseofanimals.Whereadequatepriordataexiststosubstantiatecertaintypesofsafetyinformation,theseguidelinesshouldnotbeinterpretedtomeanthattestingshouldbeunnecessarilyrepeated.1.6Thisstandarddoesnotpurporttoaddressallofthesafetyconcerns,ifany,associatedwithitsuse.Itistheresponsibilityoftheuserofthisstandardtoestablishappropriatesafetyandhealthpracticesanddeterminetheapplicabilityofregulatorylimitationspriortouse.
【中国标准分类号】:A40
【国际标准分类号】:07_080
【页数】:8P.;A4
【正文语种】:英语


【英文标准名称】:Humanfactorsdesignprocessformedicaldevices
【原文标准名称】:医疗装置人性因素设计过程
【标准号】:ANSI/AAMIHE74-2001
【标准状态】:作废
【国别】:美国
【发布日期】:2001
【实施或试行日期】:
【发布单位】:美国国家标准学会(US-ANSI)
【起草单位】:ANSI
【标准类型】:()
【标准水平】:()
【中文主题词】:设计;医疗设备;规范(验收)
【英文主题词】:Design;Medicalequipment;Medicalsciences;Medicaltechnology;Specification(approval)
【摘要】:Toprovideergonomicinformationandhumanfactorsengineeringguidancesothatoptimumuserandpatientsafety,systemsafetyandperformance,andoperatoreffectivenesswillbereflectedinmedicaldevicedesign.Specifically,therecommendedpracticedealswiththecontrols,displays,consoles,size,weight,andgeneraluserinterfacedesignofmedicaldevicesandisextensivelyillustrated.Userinstructions,manuals,software,andalgorithmsassociatedwithmedicaldevicesarealsodiscussedbriefly.
【中国标准分类号】:C30
【国际标准分类号】:11_040_01
【页数】:
【正文语种】:英语